| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6481299-6481530 | Common:4; Rare:96 | ||||
| chr11:6603597-6603815 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr11:6683266-6683652 | Common:6; Rare:145 | ||||
| chr11:8682650-8682816 | Common:2; Rare:74 | ||||
| chr11:8964372-8964518 | Common:3; Rare:46 | ||||
| chr11:9314568-9314784 | Common:2; Rare:74 | ||||
| chr11:10455135-10455280 | Common:2; Rare:25; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:10541145-10541314 | Rare:65 | ||||
| chr11:10808894-10809119 | Rare:96 | ||||
| chr11:10858030-10858237 | Common:2; Rare:58 | ||||
| chr11:11621967-11622236 | Common:4; Rare:108 | ||||
| chr11:11841950-11842008 | Common:1; Rare:19 | ||||
| chr11:14499782-14499978 | Common:3; Rare:60 | ||||
| chr11:17077618-17077893 | Common:2; Rare:118 | ||||
| chr11:17207931-17208120 | Common:1; Rare:71 |